ICON experts frequently author or contribute to industry trade press. The following are some recent articles.
2016 FDA Guidance Documents You Should Know
Gordon MacFarlane, senior manager of regulatory affairs and Cynthia Nolte, director of regulatory affairs outline the key points, benefits, and challenges of the FDA guidance documents during 2016 for medical device manufacturers.
One Answer to Your Postmarket Challenge: Planning
Interview with Vicki Anastasi on postmarket surveillance and the challenges trial designs are facing.
The Clinical Trial of the Future
Steve Cutler talks to Pharma Times regarding industry trends in clinical trials and patient engagement.
Due to considerable market growth, biosimilar clinical trials are rising in popularity.
Remote Monitoring of Patients in Clinical Trials
Recent initiatives to redesign the clinical trial process have in part focused on the creation of trials that are more patient focused.
Why Sites Matter
PMG Research contributes to this article on investigative sites and the drug development process.
Adaptive Designs for Clinical Trials
adaptive design for clinical trials and how it can improve speed to market.
Adaptive designs patient value
Adaptive design and patient value
The Patient Data Gold Rush
Tom O'Leary's presented to the Financial Times Digital Health Summit Europe regarding the use of technology to mine the clinical data patient.
Bring Your Own Device for Trial Outcome Assessment
A research survey to identify and assess the perceived barriers and challenges with the use of BYOD for eCOA in clinical trials.